30361-19-4

Usage

Chemical Properties

White Powder

InChI:InChI=1/C34H28O9/c1-34(43-32(38)26-20-12-5-13-21-26)28(41-30(36)24-16-8-3-9-17-24)27(22-39-29(35)23-14-6-2-7-15-23)40-33(34)42-31(37)25-18-10-4-11-19-25/h2-21,27-28,33H,22H2,1H3/t27-,28-,33?,34-/m1/s1

Upstream product

• 75-16-1 methylmagnesium bromide 
• 98-88-4 benzoyl chloride 
• 157037-56-4 1,3,5-tri-O-benzoyl-2-oxo-α-D-erythro-pentofuranose 
• 2747-38-8 methyltrichlorotitanium 
• 22224-41-5 1,3,5-tri-O-benzoyl-α-D-ribofuranoside 

Downstream Products

• 15397-12-3 2'-methyl-adenosine 
• 622379-83-3 C₃₀H₂₅N₃O₉ 
• 23643-36-9 2′,3′,5′-tri-O-benzoyl-2′-C-methyluridine 
• 957535-53-4 C₃₂H₂₈N₂O₉ 
• 16434-52-9 C₃₉H₃₁N₅O₈ 
• 622379-64-0 9-(2',3',5'-tri-O-benzoyl-2'-C-methyl-β-D-ribofuranosyl)-6-methylthio-purine 
• 119410-84-3 2'-C-methylthymidine 

Relevant academic research and scientific papers

2′-C-alkylribonucleosides: Design, synthesis, and conformation

Certain 2′-C-alkylribonucleotides have been designed as potential mechanism-based inactivators of ribonucleotide reductases. A short, flexible route toward the corresponding nucleosides and NMR evidence concerning their preferred solution conformations are discussed. Copyright

A concise synthesis of 2'-C-methylribonucleosides

2'-C-methylribonucleosides were synthesized in five steps from commercially available 1,3,5-tri-O-benzoyl-α-D-ribose with good overall yields.